智通财经APP讯，贝康医疗-B(02170)公布，公司的便携式精子质量分析仪于2025年 4月7日获得江苏省药品监督管理局(江苏药监局)颁发的医疗器械注册证(注册证号：苏械注准20252220581)。
据悉，公司的便携式精子质量分析仪是面向消费者端的家用活精子检测设备，专为男性生育健康设计，采用《世界卫生组织人类精液检查与处理实验室手册(第六版)》规定的精子质量检测标准。该设备小巧便捷，用户可在家中自主完成快速、准确的精子质量检测，有效规避临床检测可能带来的隐私困扰。该设备配备内置摄像头，确保每次检测图像质量稳定，避免因手机配置差异导致的结果偏差。该设备核心功能聚焦于活精子的检测与分析，可在15秒内完成数据处理，生成精子浓度与活精子活力的详细报告，帮助用户科学评估自身生育能力。未来，该设备将通过线上平台及线下实体药房同步销售，标志着公司销售渠道由专业医疗机构延伸至普通消费者应用场景。
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